Canonical Allele Identifier: PA2828577567
Gene: SPTAN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1167079
ClinVar RCV Id: RCV001515989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362243.1:p.Arg1788Lys
CA375076167
NM_001375314.2:c.5363G>A